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亚甲蓝通过 5' 腺苷一磷酸激活蛋白激酶通路诱导巨自噬来保护神经元免受血清剥夺。

Methylene blue induces macroautophagy through 5' adenosine monophosphate-activated protein kinase pathway to protect neurons from serum deprivation.

机构信息

Department of Pharmacology and Neuroscience, Institute for Alzheimer's Disease and Aging Research, University of North Texas Health Science Center at FortWorth FortWorth, TX, USA.

出版信息

Front Cell Neurosci. 2013 May 3;7:56. doi: 10.3389/fncel.2013.00056. eCollection 2013.

Abstract

Methylene blue has been shown to be neuroprotective in multiple experimental neurodegenerative disease models. However, the mechanisms underlying the neuroprotective effects have not been fully elucidated. Previous studies have shown that macroautophagy has multiple beneficial roles for maintaining normal cellular homeostasis and that induction of macroautophagy after myocardial ischemia is protective. In the present study we demonstrated that methylene blue could protect HT22 hippocampal cell death induced by serum deprivation, companied by induction of macroautophagy. We also found that methylene blue-mediated neuroprotection was abolished by macroautophagy inhibition. Interestingly, 5' adenosine monophosphate-activated protein kinase (AMPK) signaling, but not inhibition of mammalian target of rapamycin signaling, was activated at 12 and 24 h after methylene blue treatment in a dose-dependent manner. Methylene blue-induced macroautophagy was blocked by AMPK inhibitor. Consistent with in vitro data, macroautophagy was induced in the cortex and hippocampus of mouse brains treated with methylene blue. Our findings suggest that methylene blue-induced neuroprotection is mediated, at least in part, by macroautophagy though activation of AMPK signaling.

摘要

亚甲蓝在多种实验性神经退行性疾病模型中显示出神经保护作用。然而,其神经保护作用的机制尚未完全阐明。先前的研究表明,巨自噬对维持正常细胞内稳态有多种有益作用,心肌缺血后诱导巨自噬具有保护作用。在本研究中,我们证明亚甲蓝可以保护 HT22 海马细胞因血清剥夺引起的死亡,同时诱导巨自噬。我们还发现,巨自噬抑制可消除亚甲蓝介导的神经保护作用。有趣的是,在亚甲蓝处理 12 和 24 小时后,5' 腺苷一磷酸激活蛋白激酶 (AMPK) 信号通路而不是哺乳动物雷帕霉素靶蛋白信号通路被以剂量依赖的方式激活。AMPK 抑制剂阻断了亚甲蓝诱导的巨自噬。与体外数据一致,用亚甲蓝处理的小鼠大脑皮层和海马中诱导了巨自噬。我们的研究结果表明,亚甲蓝诱导的神经保护作用至少部分是通过激活 AMPK 信号通路介导的巨自噬。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/612c/3642497/abd797b97564/fncel-07-00056-g001.jpg

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